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Recent advances in the treatment of melanoma with BRAF and MEK inhibitors

机译:用BRAF和MEK抑制剂治疗黑素瘤的最新进展

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摘要

Selective inhibition of the mitogen activated protein kinase (MAPK) pathway with either BRAF or MEK inhibition has emerged as the key component for the treatment of BRAF-mutant metastatic melanoma. New evidence from several phase III trials suggests that the combination of BRAF and MEK inhibitors improves tumor response rate and progression-free survival (PFS). Some of the serious adverse events, in particular, the incidence of cutaneous squamous cell carcinoma seen with the monotherapy treatment with a BRAF inhibitor are attenuated with combination therapy, whereas milder side effects such as pyrexia can be more common with combination therapy. Although dose reductions and dose interruptions are slightly more common with combination therapy, overall data supports the notion that combination therapy is safe and improves the outcomes for metastatic melanoma patients compared to single agent BRAF inhibitors.
机译:选择性抑制BRAF或MEK抑制有丝分裂原活化蛋白激酶(MAPK)通路已成为治疗BRAF突变型转移性黑色素瘤的关键成分。几项III期试验的新证据表明,BRAF和MEK抑制剂的组合可改善肿瘤应答率和无进展生存期(PFS)。一些严重的不良事件,特别是用BRAF抑制剂单药治疗后出现的皮肤鳞状细胞癌的发生率可以通过联合疗法得到缓解,而更温和的副作用(例如发热)在联合疗法中更为常见。尽管降低剂量和中断剂量在联合治疗中更为普遍,但总体数据支持以下观点:与单药BRAF抑制剂相比,联合治疗安全且可改善转移性黑色素瘤患者的预后。

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